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The Medical Device Summer School - From Concept to CE Marking
Dec 2024
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
Dec 2024
Drafting International Commercial Agreements in English
Nov 2024
Drafting and Negotiating Clinical Trial Agreements
Nov 2024
International Conference on Islamic Studies, Law and Management (ISTILMA)
Oct 2024
Leachables and Extractables MasterClass - EU
Oct 2024
AML/CFT MasterClass - EU
Sep 2024
AI Contracting Week - with World Commerce and Contracting
Sep 2024
ESG Stress Testing MasterClass - EU
Sep 2024
Research Billing Compliance Summit
Sep 2024
Patent Protection for Software-Related Inventions in Europe and the USA
Sep 2024
Interest Rate Risk in the Banking Book (IRRBB) MasterClass - EU
Sep 2024
Key Aspects of Analytical Development MasterClass - US
Jul 2024
SOX & Internal Controls CPE Update
Jul 2024
EU and UK procedures for marketing authorisation Masterclass - US
Jun 2024
Medicare Secondary Payer (MSP) World
May 2024
Safety Data Exchange Agreements (SDEA) in Pharmacovigilance: Training Course + Workshop
May 2024
World Commerce and Contracting Negotiation Week
Mar 2024
California Meal and Rest Breaks: What You Dont Know Can Cost You
Mar 2024
Signal Management In Pharmacovigilance
Feb 2024
Transfer Pricing & Intangibles
Feb 2024
Implementation of a Successful Technology Transfer Process
Nov 2023
Tax Technology
Nov 2023
GreenTree Immigrations FREE Webinar on Canada Immigration and Permanent Residency (PR)
Nov 2023
Passport to Proficiency on the ITAR
Nov 2023
Export Administration Regulations
Oct 2023
ICD-10 Coding Updates! Effective
Sep 2023
HIPAA Business Associate Compliance and Dangers
Jul 2023
CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
Jun 2023
Responsible Business Asia
May 2023
International Conference on Human Rights and Literature
May 2023
eCTD Submissions
Apr 2023
ACFE Fraud Conference Europe
Mar 2023
Clinical Data Disclosure and Transparency Summit
Feb 2023
Digital Entertainment World (DEW)
Feb 2023
Project Management for Pharma Professionals
Dec 2022
ACFE Fraud Conference Canada
Nov 2022
International Conference on Religion and Sustainable Development (ICoReSD)
Oct 2022
Implementation of ISO 13485 MasterClass
Oct 2022
Criminal Law in Artificial Intelligence and Artificial Intelligence in Criminal Law
Sep 2022
Understanding and Managing Competition Law Compliance
Sep 2022
International Conference on Mathematics, Statistics, Education & Law (ICMSEL)
Jul 2022
International Conference on Education, Law, Business & Politics (ICELBP)
Jun 2022
Pharmaceutical Aseptic Processing Forum
May 2022
Pharmaceutical and Medical Device Ethics and Compliance Congress
May 2022
Clinical Trial Regulation MasterClass
Apr 2022
Nasal Drug Delivery
Apr 2022
Global Pharmaceutical Regulatory Affairs Summit
Apr 2022
KYOTO International Conference on `Globalization, Marketing, Management and Legal Studies` (GMMLS)
Apr 2022
HR Forum
Mar 2022
African Women Rights and their Role in Sustainable Development (AWRSD)
Mar 2022
Successfully Investigating Deviations
Mar 2022
ScaleUp 360 Smart Compliance & Tech
Mar 2022
Avoiding Pitfalls in Patent/Know-How Licences and R&D Collaborations
Mar 2022
Advanced CMC MasterClass
Feb 2022
Global Webinar on Forensic Science
Feb 2022
The EAAR Conference on New Medical Device Regulations (RMD2022)
Feb 2022
Supplier and Contract Manufacturer Management
Jan 2022
Power Project Finance
Dec 2021
FDA Pharmaceutical Labeling Boot Camp
Dec 2021
Plastics Regulations USA
Dec 2021
Aesthetic & Cosmetic Regulatory Events Summit (ACRAS)
Nov 2021
US Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors MasterClass
Nov 2021
The Art of European Claim Drafting
Nov 2021
dLaw Life Sciences Summit
Nov 2021
IP
Nov 2021
IBA Global Showcase
Oct 2021
EU Pharmaceutical Regulations & Strategy
Oct 2021
American Association of Clinical Urologists Meeting (AACU)
Oct 2021
Brand Protection Congress
Sep 2021
Facing risk in business MasterClass
Sep 2021
ACFE Asia-Pacific Fraud Conference
Sep 2021
World Commerce & Contracting Europe Summit
Sep 2021
How to submit variations in Europe MasterClass
Sep 2021
H&S Legal Compliance and Leadership MasterClass
Sep 2021
National - Strategy Summit on Paragraph IV Litigation
Sep 2021
Chemical Industry Regulations
Sep 2021
Fraud Prevention, Detection and Investigation MasterClass
Sep 2021
International Hemp Summit
Jul 2021
European Conference on Academic Integrity and Plagiarism
Jun 2021
How to Avoid Discrimination, Victimisation, Harassment and Unconscious Bias in the Workplace
Jun 2021
Employment Law in Practice from Recruitment to Termination
May 2021
Clinical Trial Supply Forum
May 2021
IBA Leadership Training Programme
May 2021
Promotional Review Committee Compliance & Best Practices Summit
May 2021
Fintech & Financing Conference and Expo (FFCON)
May 2021
AI IP Connect
May 2021
Auto IP Connect
May 2021
ScaleUp 360 Corporate Finance D/A/CH
Apr 2021
Patent Transactions
Apr 2021
The Role and Skills of a Valuable HR Assistant
Apr 2021
Nordic IPR
Apr 2021
Required New IT Security at & after Covid19
Apr 2021
LRP`s National Institute on Legal Issues of Educating Individuals with Disabilities
Apr 2021
Pharma & Biotech IP Connect
Apr 2021
SHRM Employment Law & Compliance Conference
Apr 2021
Dark Web Investigation
Mar 2021
New Medical Device Regulation
Mar 2021
Medical Writing Landscape Advancement Summit
Mar 2021
Patentability and State of the Art Searching
Feb 2021
Fraud Analytics
Feb 2021
FDA`s Medical Device Software Regulation Strategy
Feb 2021
Change Control Best Practices - Avoiding Unintended Consequences of Changes
Jan 2021
Edition Risk Data Aggregation and Risk Reporting
Nov 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
How to Conduct I-9 Self-Audits and Avoid the High Cost of Noncompliance
Oct 2020
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2020
International Conference on Pharmaceutical Regulatory Affairs and IPR
Oct 2020
Sexual Harassment Prevention 2 Day Certificate Program
Oct 2020
Project Management for FDA-Regulated Companies
Oct 2020
Risk Management in Clinical Research
Sep 2020
Virtual ISPOR-FDA Summit
Sep 2020
FDA Boot Camp Boston
Sep 2020
Virtual WFC Money Summit
Sep 2020
Transfer Pricing Professional
Sep 2020
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
Aug 2020
Life Science Regulatory Information Summit
Aug 2020
Global Conference on Disability and Islam
Aug 2020
The TID Advanced Forum on CFIUS and Foreign Investment Summit
Aug 2020
Emergence of Suicide Bomber
Jul 2020
Data Visualisation & Storytelling
Jul 2020
Effective Legal & Business Writing Masterclass
Jun 2020
Implementing a Bullet Proof Quality System for FDA Audit Success
Jun 2020
Critical Anti-Fraud Audits under Procurement and Accounts Payable
Jun 2020
FDA`s Ambitious Regulation of Social Media
Jun 2020
Gro Pro /
Jun 2020
How to Conduct an ACH Risk Assessment and Develop an Effective ACH Risk Management Program
Jun 2020
PSD 2 MasterClass
May 2020
The Workplace Investigations Masterclass – Wellington
May 2020
Contract Drafting and Negotiation in 8 Hours Masterclass
Apr 2020
Service Level Agreements Masterclass
Apr 2020
EU Medical Device Regulation (MDR) Updated CE Marking Process and ISO 13485: Expectations
Feb 2020
Statistical Analysis of Gages (Metrology)
Feb 2020
FDA Audit Best Practices - Do`s and Don`ts
Feb 2020
Audit Trail Generation and Review
Feb 2020
Contracted Services: Ensuring Compliance with the CMS Hospital CoP Standards, Joint Commission and DNV
Dec 2019
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Is the Concurrent Delay Defense Dead
Aug 2019
Effective Standard Operating Procedure (SOPs) Development
Aug 2019
HIPAA Boot Camp - Back to the Basics
Aug 2019
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Aug 2019
4-Hour Virtual Seminar on Batch Record Review and Product Release
Jul 2019
Death by CAPA Does your CAPA Program need a CAPA
Jul 2019
Workplace Unconscious Bias: Minimizing the Impact on Discrimination, Hiring, Promotions, and Retention
Jul 2019
Understanding the Most Common Violations of Law against Psychologists
Jul 2019
Payments Fraud: Detect & Prevent Check, ACH and P-Card Schemes
Jul 2019
Process Validation Requirements and Compliance Strategies
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Statistical Process Control - Keys to Prevent Process Variation and Ensure Quality
Jul 2019
Establishing FDA-Compliant Social Media Practices to Avoid FDA Actions
Jul 2019
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and How to Report It
Jul 2019
Fraud & Abuse,Stark & Anti-Kickback Issues
Jul 2019
Monitoring High Risk Transactions
Jun 2019
Top Process Validation Mistakes - And How to Avoid Them
Jun 2019
Effective Contamination Control and Environmental Monitoring Program
Jun 2019
FDA Off-Label Promotion Guidelines
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More
Jun 2019
How to Prepare Yourself for FDA`s on-going Part 11 Inspection Program
Jun 2019
Equipment Qualification and Process Validation
Jun 2019
FDA`s 21 CFR Part 11 Add-on Inspections
Jun 2019
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process
Jun 2019
Best Practices to Obtain FDA Feedback Prior to 510(k) and De Novo
Jun 2019
Bank Secrecy Act Reporting Expectations - CTRs and SARs
Jun 2019
Risk Analysis and HACCP
Jun 2019
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries
May 2019
BSA/AML Contextual Awareness of High Risk Customers
May 2019
Legal and Contractual Perspectives of Managing the Remote/Virtual Employee
May 2019
Structuring and Auditing Physician Medical Director and Administrative Arrangements: Key Stark Law Considerations
May 2019
HIPAA Compliance Monitoring and Auditing
May 2019
Overcoming Obstacles of the Canadian Drug Regulatory Landscape
May 2019
FDA Expectations for 505(b)(2) Regulatory Pathway for New Drugs
May 2019
Exploring the FDA Refuse-To-Accept (RTA) Guidance for 510(k) Submissions
May 2019
Supplier Quality Assurance Agreements: Why a General Supply Agreement Not Be Enough with Some Suppliers
May 2019
Storm Water Pollution Prevention Plans (SWPPP)
May 2019
AML High-Risk Transactions and Correspondent Banking
May 2019
How to Conduct an Internal Audit to Avoid an External One
May 2019
Texting and Mobile Devices in Healthcare - HIPAA and CMS Requirements for Security of PHI
May 2019
Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System
May 2019
Auditing Physician Contracts Under the New Stark Rules
May 2019
Dealing with the Disruptive Practitioner in a Legally Compliant Manner
May 2019
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists
May 2019
3-Hour Virtual Seminar on Best Practices to Help you Pass an FDA Computer System Validation Audit
May 2019
ISO 62304 How to Create a Medical Software Development File?
May 2019
Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance
May 2019
Legal Issues Concerning Employees with Psychiatric Illness
May 2019
How to Properly Manage a Regulatory Inspection
May 2019
The Requirements and Responsibilities of a HIPAA Security/Privacy Officer
May 2019
FDA Rules for Pharmaceutical Analytical Method Validation
May 2019
In-Depth Testing of Computer Systems Regulated by FDA
Apr 2019
Essentials of Validation - IQ, OQ, PQ
Apr 2019
Pricing Contractor Jobsite Overhead Delay Costs
Apr 2019
Continued Process Verification - A Systematic Approach
Apr 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process
Apr 2019
ANDA Submission and GDUFA Final FDA Guidance
Apr 2019
Red Flags and EDD for Non-Bank Financial Institutions
Apr 2019
Medical Device Laws and Regulations in Asia - Part 2 - India, Japan, and Korea
Apr 2019
Data Integrity: Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPR
Apr 2019
Managing the Alert/Case Clearing Investigation Process - BSA/AML/OFAC Compliance
Apr 2019
FDA Regulations & New Legislation for Marketing Cosmetics in the U.S
Apr 2019
FDA`s New Import Program for
Apr 2019
510(k) and PMA Refuse to Accept Policy
Apr 2019
Medical Device Laws and Regulations in Asia – Part 1 – China
Apr 2019
Medical Device Laws and Regulations in Asia – 2 Part Web-Series
Apr 2019
In Depth Testing of Computer Systems Regulated by FDA
Apr 2019
Supply Chain Traceability is Going Digital: What Can You do to be Prepared
Apr 2019
FDA Regulations for Pharmaceutical Current Good Manufacturing Practice (cGMP)
Apr 2019
Evolving from #MeToo – Sexual Harassment Prevention in
Apr 2019
Verification, Validation and Compliance for Medical Device Software
Mar 2019
Harmonized Tariff Schedule Classification
Mar 2019
Risk Based Monitoring for GCP Compliance
Mar 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
Anti-Kickback, Fraud, Stark, and Marketing - Where are the Landmines?
Mar 2019
EU and US GMP/GDP – Similarities and Differences
Mar 2019
FDA Regulation of Over-the-Counter (OTC) Drugs
Mar 2019
Device Changes, FDA Changes, and the 510(k)
Mar 2019
The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs
Mar 2019
Zero Acceptance Sampling to Reduce Inspection Costs
Mar 2019
FDA`s Quality Metrics - Latest Advances
Mar 2019
Selection and Use of (Certified) Reference Material in Analytical Laboratories
Mar 2019
AML/OFAC Risk Assessment – The Cornerstone of an Effective Compliance Shop
Mar 2019
FDA’s New Enforcement of 21 CFR Part 11
Mar 2019
FDA`s Scrutiny of Social Media Promotion
Mar 2019
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers
Mar 2019
The Most Serious FDA 483s - How to Avoid Them
Mar 2019
ACH 101 for Originators
Mar 2019
3-Hour Virtual Seminar on FDA`s Scrutiny of Social Media Promotion
Mar 2019
Patient Rights, Medical Records and HIPAA - What You Need to Know as a Healthcare Provider
Mar 2019
The FDA Inspection: Preparation, Management, and Follow - up
Mar 2019
Good Documentation Practices to Support FDA Computer System Validation
Mar 2019
CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture
Mar 2019
Form W-4 for : Best Practice and Compliance Requirements
Mar 2019
Criminal Background Checks in the Hiring Process
Mar 2019
FDA Regulations for Environmental Monitoring (EM) Program
Mar 2019
Mortgage Servicing Compliance: Meeting Extensive New Regulatory Expectations
Feb 2019
SR Letter 11-7 – Supervisory Guidance on Model Risk Management
Feb 2019
Fair Hearings from A Hearing Officer`s Perspective
Feb 2019
New Crystalline Silica Requirements and Strategies
Feb 2019
Form 941 for : All You Need to Know
Feb 2019
GDPR and Implications on Drug Development
Feb 2019
Introduction to Root Cause Investigation for CAPA
Feb 2019
Surviving an FDA Sponsor Inspection - Training for Success
Feb 2019
Measurement Systems Analysis
Feb 2019
Complaint Handling Best Practices - Compliance with FDA and ISO Regulations
Feb 2019
USP [1224] Transferring the Method to meet Regulatory Expectations
Feb 2019
What the US, Canada and Mexico Want from a New NAFTA
Feb 2019
Identity Issues in Banking - 26 Red Flags and More
Feb 2019
SR Letter 11-7 - Supervisory Guidance on Model Risk Management
Feb 2019
The SEC`s New Whistleblower Rules: Implications for Your Company`s Compliance and Fraud Program
Feb 2019
What FDA-Regulated Industry Should Know about FDA’s New Policy on GMP Enforcement
Jan 2019
Evolving from #MeToo: Sexual Harassment Prevention in
Jan 2019
In-Depth Computer System Validation (CSV) for FDA Compliance
Jan 2019
Step-by-Step Internal Investigations Best Practices
Jan 2019
Medical Device Cybersecurity and FDA Compliance
Jan 2019
If it Isn`t Written Down, then it Didn`t Happen: Complying with FDA`s Good Documentation Practices
Jan 2019
Drafting and Negotiating Physician Employment Contracts: Key Business, Legal, and Compensation Considerations
Jan 2019
Data Governance for Computer Systems Regulated by FDA
Jan 2019
FinCEN`s New CDD Rule - The New Prong of the AML
Jan 2019
Preventing Harassment, Abusive Behaviour, Bullying, and Discrimination in the Workplace
Jan 2019
How to Prepare for an FDA Inspections?
Jan 2019
How to prepare an Effective Audit Manual for an Internal Audit Department
Jan 2019
AML Model Validation: A Critical Need in the New Regulatory Environment
Jan 2019
Leasing Space to Physicians and Medical Groups: Knowing the Rules to Stay out of Trouble
Jan 2019
Medical Marijuana in the Workplace
Jan 2019
Strategies for Mitigating the Impact of China Tariffs
Jan 2019
Internal Controls - What Every Manager Needs to Know
Dec 2018
Resolving Construction Disputes Using Alternative Dispute Resolution
Dec 2018
Payroll in the Complicated States of California, New York, and Pennsylvania
Dec 2018
Pacing Delay - The Practical Effect on Projects and Delay Claims
Dec 2018
Handling Situations Where Regulation E and ACH Don`t Align
Dec 2018
In a Nutshell: Data Protection & Privacy Legislation in the U.S. & European Union
Dec 2018
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
How To Detect Fraud Using Excel
Dec 2018
Paying Physicians for Quality and Value: A Practical Approach
Dec 2018
2-Hour Virtual Seminar on Physician Employment Agreements, Contractor Agreements & Legally Complaint Compensation Models
Dec 2018
Developing and Implementing a Global Regulatory Plan and Strategy
Nov 2018
Medical Records: Compliance with CMS Hospital CoPs and Proposed Changes
Nov 2018
Good Documentation and Record Keeping Best Practices (FDA & EMA)
Nov 2018
Data Integrity in the Pharmaceutical Industry
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Developing an Assistance Animal Compliance Policy
Oct 2018
How to Perform a HIPAA Risk Assessment and Write Policies
Oct 2018
Auditing and examining Travel and Entertainment Expenses: Expense Reimbursement Fraud
Oct 2018
Workplace Violence Prevention Programs Including Active Shooter Scenarios
Oct 2018
FDA’s Adverse Event Reporting and Product Recalls
Oct 2018
Workplace Sexual Harassment Investigations – Best Practices
Oct 2018
Effective Batch Record Review
Oct 2018
FDA`s New Draft Guidance on Software and Device Changes and the 510(k)
Oct 2018
Structuring and Auditing Physician Employment Agreements to Comply with the Stark Law and Anti-Kickback Statute
Oct 2018
Secrets to Writing Effective SOPs for Medical Device QMS
Oct 2018
Medical Device Hazard Analysis Following ISO 14971
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Oct 2018
Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Sep 2018
FDA`s New Enforcement of 21 CFR Part 11
Sep 2018
Writing Effective Analytical Procedures
Sep 2018
System Suitability Testing (SST) for USP and FDA Compliance
Sep 2018
Chipping away at constraints – Practical tips to Improve your Manufacturing Operations
Sep 2018
FDA`s Revolutionary Change in Software Regulation
Aug 2018
How To Perform High Quality Safety Investigations
Aug 2018
HIPAA Training for Compliance Officer
Aug 2018
Understanding the HIPAA Compliance Requirements
Aug 2018
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and how to Report It
Aug 2018
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
Aug 2018
Microsoft Excel - Let`s Look Beyond the Look-Up
Aug 2018
Design Control Basics
Aug 2018
The Role of the HIPAA Security Official
Aug 2018
Deciding When to Submit a 510(k) for a Change to an Existing Device
Aug 2018
FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS
Aug 2018
Building a Compliant Documentation and Training System
Aug 2018
Seminar on HIPAA and Beyond
Aug 2018
ACH 101 for Originators: ACH Rules
Jul 2018
EHRs and Coding Errors - What Every Practice Should Know
Jul 2018
Payment Risk Management and Fraud Control
Jul 2018
Developing a Contractor Safety Program
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Practical Risk Appetite and Risk Tolerance
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Best Practices for Sexual Harassment Internal Investigations
Jun 2018
Best in Class Wage and Hour Compliance: The Federal Labor Standards Act (FLSA)
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Overtime: California Style
Jun 2018
Medicare`s New Market-Based Reimbursement System for Clinical Laboratory Testing: Tipping Point Ahead for U.S. Labs in
Jun 2018
US Expatriate Compensation Planning and Reporting Methodology
Jun 2018
Implementing Bank Secrecy Act (BSA), Audit & Best Practices
Jun 2018
Document Control and Change Control Process in GxP/GMP Environment
Jun 2018
How to prepare for a CBP Audit
Jun 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
Corrective and Preventive Action (CAPA) per FDA Requirements
Jun 2018
Off label Promotion of Drugs and Medical Devices - FDA`s Latest
Jun 2018
Environmental Compliance and Safety Management Inspection and Audit Techniques
May 2018
Is it Time to Restructure your Physician Enterprise?
May 2018
Form W-2 for : All You Need to Know
May 2018
Export Documentation and Procedure
May 2018
Employee Retention Toolkit : Set the Stage to meet Employee Expectation - Module 2
May 2018
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations
May 2018
Unemployment Claims: How to Prepare for Unemployment Hearings
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
Paying Health Care Providers for Quality and Value: Key Trends and Stark Law Considerations
May 2018
GMP Expectations for Products Used in Early Phase IND Studies
May 2018
Employers Guide to HIPAA
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
New Hire Legal Requirements and Process
May 2018
Auditing Analytical Laboratories for FDA Compliance
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
Anti-Fraud Controls in Payroll: Prevent Before It`s Too Late
May 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
Quality Management and Quality Audit According to Gxp-GMP Requirements
Apr 2018
HIPAA Risk Analysis: Clarified, Explained, Demonstrated
Apr 2018
European Data Protection Regulation - Implementation
Mar 2018
HIPAA Compliance - What you Need to Know
Mar 2018
Dietary Supplements CGMPS - 21 CFR 111 Compliance
Mar 2018
Eliminating Microbial Contamination in a Spiral Freezer
Mar 2018
Essentials of Dealing with Non-Conforming Material
Mar 2018
Bioavailability and Bioequivalence Studies Submitted in NDAs and INDs for Orally-Administered Drug Products
Feb 2018
Fundraising Under HIPAA: What You Need to Know, What You Need to Do
Feb 2018
Acceptance Activities in FDA QSR
Feb 2018
Validation of FDA-Regulated Computer Systems
Feb 2018
Compensation-Focused Compliance: Is Your Healthcare Organization Ready for Shifts in Stark Law Enforcement?
Dec 2017
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Dec 2017
FDA Regulation of Dietary Supplements
Dec 2017
FDA`s Latest Regulations for Tobacco Industry Effective 8-2016
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
New Cosmetic Product Regulation in World Economies
Nov 2017
Managing Your FDA '483' Inspectional Observations
Oct 2017
HIPAA Changes for and Beyond
Oct 2017
FDA Regulations for Analytical Instrument Qualification and Validation Processes
Oct 2017
Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices
Oct 2017
Structuring and Auditing Physician Leases Under The New Stark Rules
Oct 2017
GLP Quality System Essences and Comparison with GMP
Oct 2017
EEO-1 Form Reporting for 2018 and Trends in OFCCP Compliance
Sep 2017
1031 And 1035 Like-Kind Exchanges
Sep 2017
Title IX Training Bundle: Presidents and Study Abroad
Sep 2017
Effective Training Practices for FDA Compliance
Sep 2017
Essentials of Validation -IQ,OQ,PQ
Sep 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
New Relationship between the Data Controller, Data Processor and the Data Subject
Sep 2017
Job-Specific BSA for Deposit Operations: SAR Monitoring, 314(a) Requests & CIP
Sep 2017
Menu Labelling: Knowing the Requirements and Available Options to Achieve Compliance
Sep 2017
Stress-Testing for Financial Institutions, Beyond Regulatory Constraints
Sep 2017
Data Integrity and Its Issues
Sep 2017
Lean 5S Program - Workplace Organization
Aug 2017
Navigating the Financial Regulations of Cybersecurity
Aug 2017
Social Security - What Advisors Need to Understand Regarding Social Security When Meeting With Clients
Aug 2017
Creating a High Performance, Functional and Cohesive Team: Overcoming the Five Dysfunctions of a Team
Aug 2017
Nonresident Alien Vendors – How To Handle The Information Reporting And Backup Withholding Requirements Of The IRS
Aug 2017
FATCA (Foreign Accounts Tax Compliance Act) - How to Comply with Minimal Withholding, Tax and Penalty Impact
Aug 2017
CRE Collateral Valuation Process: Conducting a Risk Assessment
Aug 2017
FDA`s Medical Device Clinical Trials Program
Aug 2017
CMS Revised Hospital CoP Dietary, CAH Dietary, DNV Healthcare and TJC Standards
Aug 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
How to Prepare for and Host a FDA Inspection and Respond to 483`s
Aug 2017
Structuring and Auditing Physician Employment Agreements: Key Stark Law Considerations
Aug 2017
Building a Validation Program From Top to Bottom
Aug 2017
Advocacy Sanctioning: Developing Tailored Student Conduct Plans
Aug 2017
Compliance Secrets from a Former Customs Officer
Jul 2017
Pharmaceutical Quality Risk Management (QRM) Overview
Jul 2017
HUD Affirmatively Furthering Fair Housing Rule: Compliance for Governments
Jul 2017
FERPA for Faculty
Jul 2017
Personnel Training to Assure FDA and ISO Compliance
Jul 2017
FERPA Hot Topics: Big Challenges Solved
Jul 2017
Mastering U.S. Export Administration Regulations
Jul 2017
Implementing Agile in an FDA-Regulated Environment
Jul 2017
Stop Struggling with Large Word Documents: Manage with Ease
Jul 2017
ACH Fraud - Detection and Prevention
Jul 2017
Combination Products Registration
Jul 2017
USFDA Food Import and Export: Current and Future Safety Regulations
Jul 2017
Understanding Federal Government Payments
Jun 2017
Mastering HTSUS and Schedule B Code Classifications
Jun 2017
Military Lending Act Essentials
Jun 2017
OSHA 29 CFR 1910.95 - Best Practices in Implementing a Successful Hearing Conservation Program
Jun 2017
What Every Employer Needs to Know about Proposed Immigration Changes in the Trump Era
Jun 2017
` -Parties - Who are They, How To Identify Which -Party They Are, and What Are Their Responsibilities in the ACH Network?`
Jun 2017
Fundamentals of Accounting and Finance for Nonfinancial Professionals
Jun 2017
Mastering Treasury`s New Customer Due Diligence Final Rule
Jun 2017
Texting and E-mail with Patients — Meeting Patient Desires According to the Rules
Jun 2017
How to Manage the HIPAA Business Associate Process
Jun 2017
Dealing with the Weingarten Ruling (Interviewing Public Sector and Private Sector Union Employees)
Jun 2017
New California Employment Laws: Preparing for Changes to Fair Pay Act, Leave and Wage Laws, Background Checks, and More
Jun 2017
Compliance with ICH GCP R2 Addendum for Auditors
Jun 2017
FDA Policy and Goals Regarding the 483 Response
Jun 2017
Starting Your Workplace Violence Program on a Shoestring Budget
Jun 2017
Anti-Dumping and Countervailing Duties: Why, What, How
May 2017
Document Retention and Destruction What Human Resource Professionals Must Know
May 2017
ICE Audits – What All Employers Should Fear?
May 2017
How to Conduct a HIPAA Risk Assessment
May 2017
Managing a Union Represented Workplace
May 2017
Claims Adjustment Reason Codes 'CARC' and Remittance Advice Remark Codes 'RARC' Impact - How to Effectively Manage Denials
May 2017
SARs and Law Enforcement: Practical Insight to Streamline the Investigation Process
May 2017
Same Day ACH -- Credits are in Motion - Debits are Coming - How this Will change things and What`s Your Strategy?
May 2017
New FDA or EMA and USP Guidelines for Transfer of Analytical Methods
May 2017
Employment-at-Will! Does It Protect Employers from Wrongful Termination Allegations?
May 2017
How to Prepare for a Customs Focused Assessment Audit and Self Audit your Import Program
May 2017
AML Compliance and FinCEN Updates and its Implications
May 2017
Phase I GMPs
May 2017
FDA Scrutiny of Promotion and Advertising Practices
May 2017
Export Control Recordkeeping and Compliance Automation
May 2017
Employee Fraud Detection and Prevention
May 2017
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
May 2017
Sales and Use Tax - Best Practices
May 2017
Cosmetic Regulations in Major World Economies (EU, USA, Brazil, China, Japan, Korea, ASEAN)
May 2017
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2017
ISO 13485:2016 Utilizing Lean Documents and Lean Configuration
Apr 2017
Crossing the Line Online: Preventing Sexual Harassment and Sex Discrimination in the Age of Social Media
Apr 2017
Understanding and Implementing USP 1058 Analytical Instrument Qualification
Apr 2017
Cancelling Penalties and Interest
Apr 2017
Thriving with the Revised ISO 14001 Standard; Key Changes and Transition Strategies
Apr 2017
Bullying Versus Harassment: The Importance of Knowing the Difference and the Legal Significance for Employers
Apr 2017
FERPA for Advancement: Train Your Whole Shop
Apr 2017
Top 10 Ways to Get Sued From Employee Investigation
Apr 2017
Harmonized System Classification: General Rules
Apr 2017
New HIPAA Audit and Enforcement Activities: Being Prepared to Show your Compliance
Apr 2017
1099-MISC: Block By Block Discussion
Apr 2017
What You Should Know About Export Requirements for FDA Regulated Products from the US to Foreign Countries
Apr 2017
Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device
Apr 2017
New GS1 US Guideline - Pharmaceutical Industry Prepares for DSCSA Item-Level Traceability Requirements
Apr 2017
Compliance with Laws Governing Pregnant Employees and New Parents: Pregnancy at Work
Apr 2017
Identifying, Reporting and Monitoring Suspicious Activity (SAR)
Apr 2017
Preparation for GMP Inspections by Regulatory Agencies
Apr 2017
Pharmaceutical and Biologics Facility Design: FDA and Regulatory Aspects
Apr 2017
How to Detect & Prevent Expense Reimbursement Fraud and Protect Your Organization
Mar 2017
HIPAA - and the Business Associate
Mar 2017
HIPAA and Health IT
Mar 2017
Harmonized System Classification Basics, General Rules and Sections Content: Webinar Series
Mar 2017
Harmonized System Classification: Basics
Mar 2017
The 10 Step HIPAA Compliance Review
Mar 2017
Telehealth: Understanding JCAHO Standards and Legal Regulatory Compliance
Mar 2017
FDA & CFIA 2016 Regulatory Changes/Updates
Mar 2017
Structuring Physician Recruitment and Non-Physician Practitioner Support Arrangements
Mar 2017
Active Shooter Training: Preparing Your Faculty and Staff
Mar 2017
Managing an FDA Inspection
Mar 2017
Advances in Fall Protection: Guidance and Regulation for General Industry-ANSI Z359, Proposed OSHA Subpart D & I
Mar 2017
Title IX: Four Essentials for Faculty
Mar 2017
Metro 2, e-OSCAR and the New FCRA/CFPB Compliance Requirements
Mar 2017
Ransomware and HIPAA Risks - Be Very Careful Here
Mar 2017
HIPAA Changes
Mar 2017
Avoid IRS Notices By Using The Free IRS Tin Matching Program
Mar 2017
HIPAA Compliance Virtual Boot Camp
Mar 2017
Powers of Attorney: Medical Records Release Concerns
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
Microsoft Excel Series - Part 3: Beyond IF and Excel Macros
Feb 2017
Complying with `Made in USA` Labeling Standards
Feb 2017
Preparing Form 1040NR: U.S. Nonresident Alien Income Tax Return
Feb 2017
Prepare for the Unexpected - An Active Shooter Incident
Feb 2017
CUSTOMS VALUATION: How to Determine the Customs Value - Part 1
Feb 2017
HIPAA Challenges in Email and SMS Communication
Feb 2017
Contract Negotiations: Physician Employment Agreements
Feb 2017
FCPA and Anti-Bribery Cases and Trends in the US, China and Russia
Feb 2017
The HIPAA Privacy Rule - What You Need to Know as a Healthcare Provider
Feb 2017
Spotlight on Post Market Surveillance
Feb 2017
EE0-1 Reporting Form Changes in and How Company`s Can Be Compliant
Feb 2017
Microsoft Excel Series - Part 2: Learn More about Macros
Feb 2017
How to conduct a Human Factors and Usability validation following ISO62366 and the new FDA Guidance
Feb 2017
How to Determine Which Jurisdiction`s Employment Laws Reach Border-Crossing Staff
Feb 2017
The NAFTA (Canada, Mexico, US) Rules of Origin and Certificate of Origin Requirements
Feb 2017
Techniques to engage information workers to improve Information Governance compliance
Feb 2017
New Fatca & Fbar Filing Requirements: Meeting the Requirements and Avoiding the Penalties
Feb 2017
OSHA Inspections - Avoiding the Most Common Mistakes
Feb 2017
The Basics of Professional Regulatory Law: Licensure and Certification, with an Emphasis on Health Professions
Feb 2017
Risk Management for Non-Student Minors on Campus
Jan 2017
California Prop 65 - New Article 6 Regulations for Clear and Reasonable Warnings: What you need to Know?
Jan 2017
The DOJ Gets Personal: 6 Things You Should Know About the Yates Memo
Jan 2017
Countdown to Compliance Under OSHA`s Final Silica Rule: Best Practices for Developing a Written Exposure Control Plan
Jan 2017
Chemistry 101 for Medical Device Regulatory & Quality Professionals: Essential knowledge needed to Manage Drug&Device Combination Product Project
Jan 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
FDA Regulation of Combination Products
Jan 2017
IRS Tax Codes: Form W-2 or Form W-2c, Form W-4, Form SS-8, Forms 940 and 941
Jan 2017
How to Write HIPAA Policies and Procedures
Jan 2017
FDA Food Labeling Claims - Understanding the Advantages and the Risks of Claims
Jan 2017
On-site BSA/AML/OFAC Examination
Jan 2017
Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements
Jan 2017
You’re Hired! The Ins and Outs of Negotiating and Drafting Physician Employment Agreements
Jan 2017
Implementation of the Generic Drug Labeling Rules
Jan 2017
The New FDA-Product Approval, Inspection, and Enforcement
Jan 2017
National Consumer Assistance Plan
Jan 2017
Judicial Imperative for Mitigating Recalls and Outbreaks in Food Industry
Jan 2017
Vendor Management Program - Risk Assessment, Effective Controls, Best Practices to Minimize 3PV Risk
Jan 2017
What the FDA FSMA Transportation Rules Mean for U.S. Food Importers and Foreign Suppliers
Jan 2017
FDA Warning Letter - Consent Decree Software Validation
Jan 2017
Fundamentals of the de novo process for medical devices: What you need to know when pursuing a de novo application and approval with the FDA
Jan 2017
Legally Terminating Employees: 10 Critical Things you must Know
Dec 2016
Lean Healthcare Facility Design
Dec 2016
21 CFR Part 11 - Electronic Record and signature Validation
Dec 2016
Awareness of Potential Food Safety Problems that Occur During Food Transportation (2)
Dec 2016
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation
Dec 2016
Workplace Violence Then and Now: 25 Years of Threat Assessment and Management
Dec 2016
Preventing Corporate and Governmental Fraud
Dec 2016
When Regulation E and ACH Don`t Align
Dec 2016
Quality and Compliance - Building Your Key Capabilities for Future Success
Dec 2016
Clinical Evaluation Reports (CER`s) Required for All Medical Devices in Europe
Dec 2016
Application of CMS Quality Indicator Process in Healthcare Food Service
Dec 2016
ERISA Essentials for Lawyers, Employers and HR Professionals
Dec 2016
FDA Action on Antiseptic Wash Products: What is Next for the Industry?
Dec 2016
Using US Customs FREE ACE Portal to Improve Import Compliance & Identify Strategic Opportunities
Dec 2016
Understanding the Mexican Standard NOM-086-SSA1-1994 for food and beverages with modifications in its composition
Dec 2016
2017 NACHA Operating Rules Preview and Update on Rules
Dec 2016
Product Risk Management Under ISO 14971:2007 and ICH Q9
Dec 2016
Go Beyond ISO 9001:2015`s Requirements when Dealing with Risk
Dec 2016
Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
Dec 2016
Fundamentals of Oil & Gas Agreements
Nov 2016
Challenges of Change Control: Implementation and Maintenance
Nov 2016
Effective Complaint Handling & Medical Device Reporting
Nov 2016
Title IX and Study Abroad: Planning for Success
Nov 2016
Understanding European Filing and Registration Procedures for Drug Approval
Nov 2016
Compliance with the European Cosmetics Products Regulation (EC) 1223-2009
Nov 2016
The OCR Phase 2 Audit Program
Nov 2016
Overview of the Mexican Labeling Standards and the New Labeling Requirements
Nov 2016
Preparing for the Upcoming EU Medical Device Regulations
Nov 2016
Social Media Policies: Risks and Regulations
Nov 2016
Responsibilities of the HIPAA Privacy Officer - Ensuring Compliance and Avoiding Penalties
Nov 2016
Phase 2 HIPAA Audits: What to Expect and How to Pass
Nov 2016
HIPAA Security & Privacy Risk Analysis- OCR Audits
Oct 2016
The Office of Federal Contract Compliance Programs (OFCCP) Finally Updates Their 1970 Sex Discrimination Guidelines: What You Need to Know to Reduce Liability- Susan Strauss
Oct 2016
How to conduct a HIPAA Security Risk Assessment and Write Policies-Brian L Tuttle
Oct 2016
Application for Investor Advisor Registration - ADV Part 1, Part 2A, Part 2B and More
Oct 2016
Mandatory GMO Labeling: Preparing for Implementation
Oct 2016
Remote Deposit Capture (RDC) Rules and Regulations - Legal and Compliance Requirements
Oct 2016
Understanding E-banking Compliance Regulations
Oct 2016
FDA’s New Draft Guidance on Data Integrity for CGMP Compliance
Oct 2016
Understanding the Impact of the Americans with Disabilities Act Amendments Act (ADAAA)- Steering Clear of Liability
Oct 2016
Adverse Event Reporting - Best Practices Dietary Supplements
Oct 2016
From Volume to Value: An Overview of MACRA, MIPS, APMs and the New CMS Quality Payment Program
Oct 2016
Federal Tax Update: Individuals (Form 1040)
Oct 2016
Substantiation of Food and Supplements Marketing Claims: FDA and FTC Requirements
Oct 2016
Tax Refund Frauds: Personal and Business Identity Theft
Oct 2016
Preparing for and Defending Against a Customs Audit
Oct 2016
PCI DSS Compliance in Advancement: Update for 3.2
Oct 2016
What to Do When the DOT Hazardous Materials Enforcement Inspector Comes Knocking
Oct 2016
Acceptance Activities in FDA QSR
Oct 2016
Bank Secrecy Act & Beyond: Understanding Currency and Monetary Reporting Requirements
Oct 2016
FDA Vs Health Canada
Oct 2016
New DOL Regulations on Salaried Exempt Employees
Oct 2016
Learning Design Controls through Review of FDA 483 Observations
Oct 2016
How to Use Big Data for AML/AB&C Compliance and Risk Mitigation
Oct 2016
Preparing Managers for Layoff Communication: Practical Strategies for Notifications and Beyond
Oct 2016
Chemical Safety for the Century Act
Oct 2016
Understanding Proper Labeling & Packaging Requirements & How to Stay Legally Compliant
Oct 2016
How to Conduct an Effective Annual Product Quality Review
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
The Disruptive Practitioner: A Danger to the Hospital`s Operation
Sep 2016
Fake Checks & Counterfeit Currency
Sep 2016
FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready?
Sep 2016
GCP: The IND, How to Gain Approval for Clinical Trials in the USA
Sep 2016
FDA Regulations for Marketing Dietary Supplements in the U.S
Sep 2016
Child and Spousal Support (Part I)
Sep 2016
What to Expect in a Federal HIPAA Audit & How to Avoid a Federal Audit
Sep 2016
Regulatory Document – Site Master File
Sep 2016
Quality Metrics Program: FDA Challenges and Requirements including the New `Quality Metrics Technical Conformation Guide` Released
Sep 2016
Global Focus: A Guide to Identifying PEPs and Meeting Anti-Bribery and Corruption Obligations
Sep 2016
International Visas and How Payroll Should Handle Them
Sep 2016
Business Law Basics and Lender Liability - How the Legal System Can Help You and How You Can Avoid a Lawsuit
Sep 2016
Good Documentation Practice for GxP Environments
Sep 2016
Understanding Pay Equity, Discrimination and Reporting Requirements
Sep 2016
How to Avoid PHI Breaches and HIPAA Violations While Doing Patient Engagement through Websites, Marketing and Social Media
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
Identifying Beneficial Owners and Control Parties for Business Accounts
Sep 2016
How to avoid misclassification: Independent Contractor (Self-Employed) or Employee?
Sep 2016
FDA`s Pet Food Labeling Guidelines
Sep 2016
Negotiating Your Contracts Tricks to the Trade
Sep 2016
Estate Planning for and Beyond
Sep 2016
IRS Enforcing Due Diligence Rules against Return Preparers
Sep 2016
FDA and CFIA-Overview of Proposed Regulations - Let`s Get Updated
Sep 2016
Defining and Managing Protocol Deviation/Violation/Exception
Sep 2016
Title IX and Protecting the Rights of the LGBTQ+ Community on Your Campus
Sep 2016
Registering Your Brand Name and Logo with the USPTO
Sep 2016
ASQ Certified Quality Engineer (CQE) Exam Preparatory Course - Webinar Series
Sep 2016
Successfully Avoiding and Defending against Unemployment Claims
Sep 2016
Medical Device Tracking: Latest FDA Update and Expectations
Sep 2016
Get ready for your HIPAA Compliance Audit
Sep 2016
Subordinated Debt Financing from Non-Profit Lenders
Sep 2016
FDA Regulation of Digital Health - Current Status and Recent Developments
Aug 2016
Business Continuity or Disaster Recovery Planning
Aug 2016
Accelerated Aging Product Testing
Aug 2016
Deemed Exports under the EARs
Aug 2016
Why use IRS e-services TIN Matching Program
Aug 2016
Logistics Channel Incoterms Standards
Aug 2016
Cuba Sanctions: All You Need To Know
Aug 2016
Internship Programs: Limiting Potential Liabilities
Aug 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Changes to the Common Rule (45 CFR 46) : What this means for you
Aug 2016
Challenges of the and Week Payrolls and How to Overcome Them
Aug 2016
Employee Leave Abuse (FMLA & ADA/ADAAA)
Aug 2016
Cyber-Crime : The Internal and External Threat to You and Your Organization
Aug 2016
How to do a Risk Analysis
Aug 2016
Regulatory Update: FINCEN`s New CDD Rule and the New Prong of the AML Program
Aug 2016
COSO Integrated Guidance: Effective Internal Control for Successful Corporate Management
Aug 2016
Customs-Trade Partnership Against Terrorism (C-TPAT) and Supply Chain Security
Aug 2016
Health Care Reform - New and Current Issues Regarding the Affordable Care Act (Obamacare)- Part 2
Aug 2016
FSMA Gives FDA Recall Authority Over Adulterated Food and Broadens Standards for Food Detention
Aug 2016
How to Prepare for Increased HIPAA Enforcement
Aug 2016
Interpreting and Reporting Descriptive Statistics
Aug 2016
Mastering Negotiation Skills: Win-Win Tools to Advance Your Business Objectives
Aug 2016
New CMS CoP Regulations for Managing Grievances and Complaints: What Hospitals Should Know about the CMS and Joint Commission and DNV Standards
Aug 2016
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs
Aug 2016
Are You Ready For The FDA`s Mandate Requiring Electronic Submission Conformance to SEND and SDTM?
Aug 2016
Medical Staff Bylaws Requirements For Joint Commission Accreditation
Aug 2016
Considerations for a Successful Biosimilars Program
Jul 2016
Bullying Versus Harassment: Understanding the Difference and Protecting Yourself from Both
Jul 2016
Risk Assessment and Business Impact Analysis using PMI and ISO/IEC 21500 Project Management Methodologies
Jul 2016
Health Canada`s Regulations on Natural Health Products vs. FDA`s Dietary Supplement Regulations
Jul 2016
The Underproductive Lawyer: Addressing Performance Issues in Law Firms
Jul 2016
340B Compliance and Self audits
Jul 2016
How to Conduct a Human Factor Analysis of Instructional Documents, Particularly Master Batch Records (MBR) and Standard Operating Procedures (SOP)
Jul 2016
FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings
Jul 2016
You Said Whaaat? Limiting Employer Liability for Sexual Harassment in the California Workplace
Jul 2016
SharePoint Governance for the End User Community
Jul 2016
The JOBS Act - The Regulation D Offering Reborn
Jul 2016
Title 19 Customs Duties Parts 200 to End, Revised
Jul 2016
Proper CAPA Management and Root Cause Analysis
Jul 2016
Process Validation - Current Industry Practices and FDA Guidance Document Review
Jul 2016
Overview of the Foreign Corrupt Practices Act
Jul 2016
Overview of FDA Regulation of the Tobacco Industry
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
Set-Up of Insurer Bad Faith, Defense of Bad Faith Suits
Jun 2016
Writing Effective Environmental Impact Statements (EIS) Under National Environmental Policy Act (NEPA)
Jun 2016
OSHA Recordkeeping: What to Save, What to Delete, and Everything In-Between
Jun 2016
Process for Performing a Vendor/Contract Audit: What Should be Considered and How to Plan, Perform and Report Results of a Vendor Audit
Jun 2016
Lending Compliance Update
Jun 2016
IRS Update
Jun 2016
Comparison of GFSI with FSMA requirements
Jun 2016
Universal Design: Proactively Addressing Accessibility on Campus
Jun 2016
Understanding and Implementing the EU Vigilance System
Jun 2016
Loan Portfolio Management and Review - Regulations, Process, Loan Grading Techniques, Collateral and Documentation
Jun 2016
Background Checks in California: Best Practices for Hiring in the Golden State
Jun 2016
Alternative Withholding Methods: Income Tax Computations for Special Situations
Jun 2016
The Past Isn`t in the Past`: Effecting Sound Employment Background Checks in California
Jun 2016
FDA`s Low-Risk Device Policy and the Impact on Mobile Medical Device Applications
Jun 2016
Gluten-Free Labelling with a Special Focus on Fermented, Hydrolyzed or Distilled Foods: How to Prove & Display It Correctly
Jun 2016
Compliance with U.S. Securities and Exchange Commission Laws
Jun 2016
Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance
Jun 2016
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods
Jun 2016
Mexico Maquiladora/IMMEX and their Free Trade Agreements
Jun 2016
Performing Anti-Fraud Audits in Purchasing and Accounts Payable
May 2016
Copyright for Online Course Materials
May 2016
Legally Compliant Employer-Employee Arrangements: Non-Compete Agreements, Classifying Independent Contractors vs. Employees, and Employment-Related Contracts
May 2016
Mastering Customs Classification Under the Harmonized Tariff Schedule
May 2016
GMPs for OTC and Cosmetic Products - US and Global Requirements
May 2016
Implementing Advanced Pivot Table Techniques
May 2016
CMS Proposed Changes to the Discharge Planning Standards and the IMPACT Act
May 2016
Payroll Recordkeeping Compliance
May 2016
Lifecycle Approach to Analytical Methods: Incorporating QbD Principles into Method Development, Validation and Transfe
May 2016
Advertising and Promotional Material Compliance and Review Process
May 2016
Medicare Penalties and Incentives- Updates for Medical Practices
May 2016
Key Factors to Develop HIPAA Policies and Procedures
May 2016
Final FSMA Subpart G Rule Requirements for the Receiver Liability for Supplier Preventive Controls
May 2016
Advanced Consumer Lending - Process, Best Practices, 6Cs of Credit, Loan Structuring and Pricing
May 2016
Importing Marketing Channel Audits
May 2016
Legal Hiring and Termination
May 2016
Final revised Draft to ISO 14644 Parts 1 and 2 changes Classification and Monitoring Methods: Are you prepared?
May 2016
Understanding Disclosures, Certifications and Corporate Responsibility Relating to SOX - Sections 302, 401, 404, 409, 906
May 2016
GMP Complaint Systems and Product Recalls
May 2016
I`m Out`a Here! Successfully Navigating the California Family Rights Act (Part – I)
May 2016
Implementing Validation and Qualification - Annex 15 and FDA Requirements
May 2016
Evolution of Board Responsibility for Compliance Program Oversight
Apr 2016
USP [800] - Guidelines for Safe Handling of Pharmaceuticals
Apr 2016
The Trans-Pacific Partnership: Opportunities & Risks
Apr 2016
Best Practices for Compliance with FDA 21CFR1040
Apr 2016
3 Ways to Avoid Costly Wage and Hour Problems
Apr 2016
FDA NLEA Regulation for Retail and Foodservice Labeling - An Overview of Current Regulation and Pending Regulations
Apr 2016
Do`s and Don`ts of Effective HIPAA Compliance program for BYOD & Mobile Devices: Be Prepared for what`s new in !
Apr 2016
Non-Resident Employee Tax Withholding
Apr 2016
Staying in Compliance with the Federal Debt Collection Practices Act (FDCPA): What Debt Collectors can Say or DO?
Apr 2016
Elemental Impurities: The New Requirements
Apr 2016
Packaging and Labeling for Commercial and Clinical Products
Apr 2016
FDA New Electronic Data Capture Guidance - What is the impact on Inspectional Record Requirements
Apr 2016
How the FDA & FTC Regulate Advertising & Promotion of Drugs & Dietary Supplements
Apr 2016
The New Clinical Trial Regulation
Apr 2016
How Fixing FDA Compliance Problems (Remediation) Aligns with the 5 Stages of Grief
Apr 2016
What Practitioners need to know about the difference in Ethics and Law for Mental Health Professionals
Apr 2016
Employee Settlement Agreements in : Make Sure You Get Them Right - FLSA, EEOC, ADEA & NLRB
Mar 2016
The Federal False Claims Act and the Anti-Kickback Statute: Is Your Organization at Risk
Mar 2016
Evaluating the Effectiveness of a Corporate Compliance Program
Mar 2016
Introduction to Country of Origin: Essential Practices for Import Management
Mar 2016
FMLA, ADA, USERRA, Workers Compensation, and HIPAA : Navigating the Bermuda Triangle of Medical Leaves
Mar 2016
Optimizing Target Weights for Foods and Beverages
Mar 2016
Ensuring Compliance of Your Bioanalytical Method Validation with the 2013 FDA Draft Guidance
Mar 2016
Office of Inspector General (OIG) Work Plan : Trends, Reports and Issues
Mar 2016
Obligations, Responsibilities and Warranties of the RDFI and ODFI for Special Processes: Returns & NOCs - the RDFI processes-Part 1
Mar 2016
Top Violations of Law Committed by Physical Therapists. What did I do wrong
Mar 2016
Top 10 ACA Traps for the Unwary - What you should know about The Affordable Care Act (ACA) before the Reporting Deadline
Mar 2016
AML Investigations and SAR Preparation
Mar 2016
How to Apply ISO 27001 Principles to Enterprise Risk Management in
Mar 2016
DOL`s New Proposed Overtime Pay Regulations & Proposed Rules - What to Expect and How to Comply
Mar 2016
Auditing Hospital-Physician Arrangements & Contracts under the New Stark Rules
Mar 2016
HR and the Law : Ensure Policy Meets Practice
Mar 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
Trade Measures and WTO
Mar 2016
Confined Space Entry Regulation Requirements
Mar 2016
The importance of Detecting Truth, Deception, and Lies while conducting an Investigative Interview
Mar 2016
Device Changes and the 510(k)
Mar 2016
Understanding Incident-To Compliance
Mar 2016
Highest Risk Factors for HIPAA Violations
Mar 2016
Shooting and asking Questions Later: How A Health Care Practitioner can Lose their License Immediately on the Spot
Mar 2016
How to Avoid and OCR HIPAA Audit
Feb 2016
Building an effective AML Program and Best Practices for Sanctions Screening
Feb 2016
Guidelines for Performing Fraud Risk Assessment and How to Conduct an Internal Fraud Investigation
Feb 2016
Root Cause Analysis - The Heart of a Successful CAPA Program
Feb 2016
Auditing Physician Contracts Under the New Stark Rules
Feb 2016
The CMS Restraint and Seclusion: Navigating the Most Problematic of all of the CMS Standards
Feb 2016
Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited
Feb 2016
Creating Effective SOP for Regulatory Compliance
Jan 2016
Stress-Testing for Financial Institutions, Beyond Regulatory Constraints
Jan 2016
Prevention of Sexual Harassment
Jan 2016
Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico
Jan 2016
Payroll Technology
Jan 2016
How to Develop a strong CAPA System by Understanding its Unique Challenges
Jan 2016
Managing Student Activism
Jan 2016
Controlling Human Error in the Manufacturing Floor
Jan 2016
All You Need to Know About Same Day ACH - Faster Payments!
Jan 2016
Social Media as a Recruiting Tool: Strategies for Using Facebook, Twitter, and LinkedIn
Jan 2016
Good Social Media Practices to Avoid FDA Actions
Jan 2016
Preparation is the Best Medicine: Getting Ready for OSHA`s New Strict, Expanded Enforcement against the Healthcare Industry
Jan 2016
Cleanroom Monitoring & Maintaining a Quality Environment : Overcoming USP [797] Common Non-Compliance Issues
Jan 2016
Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820
Jan 2016
FSMA Final Rules for Preventive Controls for Human and Animal Food
Jan 2016
Established Condition - The New FDA Guidance
Jan 2016
Trends in U.S. Payments Landscape - Tokenization, EMV/NFC and How it Affects Merchants Accepting Payments
Jan 2016
Drug Master Files: New Implications under GDUFA
Jan 2016
Intro to Government Contract Proposals
Jan 2016
The HIPAA HOT List: Key Issues in HIPAA Compliance Today
Jan 2016
Social Media Risks, Rules, Policies and Procedures: Best Practices to Minimize Risks, Manage Use and Maximize Legal and Regulatory Compliance
Jan 2016
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2016
Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs
Jan 2016
Implementing the ACA, HIPPA, and Discrimination Laws into Your Organization`s Wellness Strategy
Jan 2016
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Jan 2016
AML/OFAC Risk Assessment: The Cornerstone of an Effective Compliance Shop
Jan 2016
Statistical Process Control
Jan 2016
Usability Engineering in IEC 62366-1:2015 - Implementing the New Standard
Jan 2016
FDA Inspections : Managing the Myth and the Reality
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
Last Minute Update: Hidden Changes to 2015 and Income Tax and Information Reporting Forms
Jan 2016
Construction Claims - Keys to Preparation
Jan 2016
Bulletproof Workplace Investigations
Jan 2016
Risk Management and Risk-Based Monitoring
Jan 2016
Creating and Maintaining a GMP Quality System
Jan 2016
Auditing Physician Contracts Under the New Stark Rules
Jan 2016
How to Identify, Investigate, Deny and Terminate FMLA Abuse
Jan 2016
Environmental Monitoring: Prepare Your Company to Meet Final FSMA Rule Requirements
Jan 2016
Process Robustness: The New FDA Paradigm
Jan 2016
How to Detect Lack of Data Integrity
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
Incorporating Risk Management into Process Improvement
Jan 2016
Establishing a Service Level Agreement (SLA) Process
Jan 2016
FDA Compliance and GAMP V Computer System Classification
Jan 2016
Writing Effective Standard Operating Procedure (SOPs)
Jan 2016
How to Respond to an FDA Investigation: What happens when the FDA threatens to shut you?
Jan 2016
Complaint Handling Requirements - Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities
Dec 2015
New HIPAA Audit and Enforcement Activities: Being Prepared to Show your Compliance
Dec 2015
Exempt v. Nonexempt: Ensuring Proper Classification of Employees for Compliance with Federal Overtime Laws
Dec 2015
Fraud Incident Response Plan
Dec 2015
Paediatric Drug Development - Adult Data and Relevant FDA Laws
Dec 2015
The Impact of Basel III on Export Finance
Dec 2015
Changing Trend in Risk Allocation - Differing Site Conditions
Dec 2015
Law Enforcement Techniques - Identify Threats, Manage Crises and Spot Concealed Carry
Dec 2015
Sales Tax - Avoiding Double Taxation on Drop Shipments
Nov 2015
HIPAA Compliant Patient Engagement: New Rules on Email and Text (SMS) for Health Care Providers and Business Associates
Nov 2015
Ensure Compliance to FDA`s Design Control Requirements using Requirements Management Techniques
Nov 2015
Effective Quality Audits: Digging Deep
Nov 2015
Computer System Validation for Systems Supporting Clinical Trials
Nov 2015
Corrections and Removals - Understanding and Implementing the Final Guidance Document
Nov 2015
Audit program (Internal & External) for Clinical trial sites
Nov 2015
Reducing your Exposure to a GMP FDA Warning Letter
Nov 2015
Banking and Marijuana: When Federal and State Laws Collide
Nov 2015
AML High-Risk Transactions - Identifying and Managing Them
Nov 2015
ICH-FDA Good Clinical Practice – Managing Clinical Trials
Nov 2015
Current Legal and Regulatory Challenges for HR
Nov 2015
Best Practices For Preparing For an ISO Audit
Nov 2015
Due Diligence - Quality and Compliance Aspects for Medical Devices
Nov 2015
Confined Space Rules for Construction that are in the Final OSHA Rule
Nov 2015
Building a Vendor Qualification Program for FDA Regulated Industries
Nov 2015
Title IX: 5 Things Every Department Chair Needs to Know
Nov 2015
FDA New Electronic Data Capture Guidance- Inspectional Record
Nov 2015
Business Plans That Get Results
Oct 2015
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Oct 2015
Risk Based Approach to Software Quality Validation
Oct 2015
Technology/Analytical Method Transfer
Oct 2015
Drug Product-Injury Litigation: Effective Use of Medical Information and the Scientific Literature in Building a Strategy for Defense
Oct 2015
Fringe Benefit Taxation and IRS Compliance
Oct 2015
A look at 510(k) changes
Oct 2015
Ethics for Litigation Attorneys
Oct 2015
Impact on Exporters of Foreign Assets Control, Anti-Boycott and Anti-Money Laundering Regulations
Oct 2015
Procure-to-Pay Fraud Cycle: Detecting and Preventing Purchasing, Receiving and Disbursement Frauds
Oct 2015
Supply Chain Profitability - Achieve Competivitive Edge by Reducing Costs & Improving Performance
Oct 2015
Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration
Oct 2015
Complying with SSA and IRS Rules for Correcting Forms W-2 and 941
Oct 2015
Ethics for Transactional Attorneys
Oct 2015
Changes under the HIPAA Omnibus Rule - What`s New
Oct 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
Dealing with the IRS and Other Government Agencies
Sep 2015
Operational Risk for Financial Institutions - Beyond Regulatory Constraints - By Compliance Global Inc.
Sep 2015
The Logistics and Law of Exporting from the United States
Sep 2015
Seven Step Compensation Diet
Sep 2015
FDA Inspections: Preparation and Managing the Consequences
Sep 2015
California Laws- Pregnancy Disability Leave- Ban the Box
Sep 2015
US Drug Supply Chain Security Act - Serialization & Validation for Track & Trace Compliance
Sep 2015
Calibration and Qualification in Analytical Laboratories
Sep 2015
How can Vendor- Sponsor Collaborate to Deliver a Quality Service
Sep 2015
Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration
Sep 2015
Health Care Reform and Review of Affordable Care Act Requirements
Sep 2015
FDA 510(k) Requirements, Submission, and Clearance: Best Practices
Sep 2015
Application of Lean Six Sigma Methodology for Regulated Industries
Sep 2015
Regulatory Expectations-Best Practices in Asset Liability Management
Sep 2015
Highest Risk Factors with HIPAA
Sep 2015
When is Overtime Pay Required- FLSA Regulation
Sep 2015
Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions
Sep 2015
Fraud 101 for Compliance Professionals: Current Compliance Policies and Procedures
Sep 2015
The Anti-Kickback Statute: Paying for Referrals is a Bad Idea
Sep 2015
CLOs - Analysis of Lenders
Sep 2015
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process
Sep 2015
Managerial Primer for Assuring IT Legal Compliance
Aug 2015
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors
Aug 2015
Sanitary Food Packaging Concepts-Food Safety Training
Aug 2015
Regulatory Inspection at Your Food Facility- Food Safety Guidelines
Aug 2015
Proper Handling of Payroll Overpayments
Aug 2015
Patients Suing Under HIPAA: Beware of New Laws and Risk
Aug 2015
ISO/FDIS 9001: - Planning for the Changes
Aug 2015
Increasing Margin through Trade Compliance-How To Cut Cost
Aug 2015
Banking Regulations -, Federal Banking Regulations
Aug 2015
The Federal False Claims Act: Enforcement and the Obamacare Expansion
Aug 2015
Orphan Drugs: the Conundrum- Clinical Research Trials
Aug 2015
Training in Regulated Environments- Regulatory Compliance Training
Aug 2015
Creating a Global Regulatory Plan
Aug 2015
Understanding ISO 13485-FDA Requirements for Medical Devices
Aug 2015
Trends in Audit, Risk, and Compliance: Integrating your “ARC”
Aug 2015
System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
Recoupment for Unsupported Services and Failure to Balance Bill Out of Network Patients—What’s Your Best Defense?
Aug 2015
Legal and Effective Behavioral Interviewing
Aug 2015
Understanding FDA Regulations and Role in Opioid Pain Management
Aug 2015
CDOI, 790.03(h): The California Fair Claims Settlement Practices Regulations
Aug 2015
Failure Mode and Effects Analysis for Design Improvement and Design Control
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
Export to Mexico Documentation & Procedures
Jul 2015
How To Avoid FDA 483’s/ Warning Letters? What to Do If You Happen to Get One?
Jul 2015
Paediatric Drug Development - Adult Data and Relevant FDA Laws
Jul 2015
B2B Payments -Compliance Issues Faced in
Jul 2015
Avoid IRS Form Issues, Stay Updated
Jul 2015
Top 10 Contract Killer Clauses: How to Negotiate Out of Them
Jul 2015
FDA Inspection and Medical Device Design Control
Jul 2015
Tips for creating Social Media strategy and policy
Jul 2015
E-Compliance: Know Your Internet rights- Cyber Security Laws
Jul 2015
FERPA Essentials for Faculty
Jul 2015
Conducting Effective FMEA to address JCAHO Requirements
Jul 2015
Validation of Complex Cell-Based Potency Methods
Jul 2015
Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices
Jul 2015
Canadian Site Licence Applications for Dietary Supplements. - By Compliance Global Inc
Jul 2015
Canadian Product Licenses for Dietary Supplements. - By Compliance Global Inc
Jul 2015
HIPAA Fundraising Strategies: Compliant, Proper use of Protected health Information. - By Compliance Global Inc
Jul 2015
Internal Investigations: The Role of Documents in the Investigation
Jul 2015
OSHA Enforcement for Employers Using Temporary Workers
Jul 2015
Understanding Employee’s Nationalization Status for Purposes of Payroll
Jul 2015
Computer System Validation to Mobile Applications-Live Training
Jul 2015
CDOI: Compliance with the California SIU Regulations
Jul 2015
Business Frauds: Detection, Prevention and Controls
Jul 2015
A+ on Retaliation Claims Compliance: Deal with the problems In House rather than in the Court House
Jul 2015
Drug Diversion by Healthcare Personnel -Prevention Program to Protect Your Patients, Employees, and Organization
Jul 2015
Expense Reimbursement Fraud: Detection, Prevention and Deterrence
Jul 2015
Canadian Establishment Licenses: Drugs, Supplements and Medical Devices
Jul 2015
Using Q-Submission to Most Effectively Prepare for an FDA 510(k) Submission
Jul 2015
Simple Substantial Economic Effect Regulatory Compliance
Jun 2015
Employee’s Nationalization (Resident and Non Resident) Status for Purposes of Payroll
Jun 2015
McNamara-O’Hara Service Contract Act-Online Training
Jun 2015
Normality Tests and Normality Transformations
Jun 2015
Treasury Management - Liquidity, Interest Rate, Foreign Exchange and Capital Risk Management
Jun 2015
Bloodborne Pathogen
Jun 2015
International Product Registration: What documents are required?
Jun 2015
Writing Evaluation Reports-How to Write Evaluation Report
Jun 2015
U.S. FDA`s New Strategic Priorities 2014 - 1018 ()
Jun 2015
Manage Your FDA Inspection Before It Happens
Jun 2015
Travel Pay: Handling it Correctly
Jun 2015
Civil Monetary Penalties-Civil Monetary Penalties Law
Jun 2015
The Ultimate Guide to Navigating California Medical Leaves: The Ultimate Guide to PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA and Workers Compensation
Jun 2015
A+ Compliance with Pregnant Employees and New Parents: Pregnancy at Work
Jun 2015
Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
Set-Up of Insurer Bad Faith, Defence of Bad Faith Suits and `Reverse Bad Faith` Claims: Insurer vs. Policyholder Perspectives
Jun 2015
OSHA - 10 Major Differences between Federal OSHA and California OSHA Compliance and Enforcement
Jun 2015
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices
Jun 2015
Administrative Law in Professional Licensing Actions
May 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Best Practices - Using Ratios for Fraud Detection in Corporate Revenue Accounts
May 2015
California Laws Regulating Employment Screening and Safe Hiring
May 2015
The Canadian Food Label
May 2015
Best Practices for Preparing for a Technical File for CE Mark
May 2015
CAPA, Failure Investigation and Root Cause Analysis - FDA Expectations
May 2015
Ensuring Data Integrity for FDA/EU Compliance
May 2015
Understanding the New Custom Device Exemption Guidance
May 2015
Managing FDA After a Bad Inspection
May 2015
Complying with Section 702 of the Choice Act
May 2015
Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR
May 2015
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
May 2015
Part 2 - Quality Management System effectiveness: ICH Q10 principles, impact of failure on COGS, principles of QRM, what you can impact in reactive versus proactive
May 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
May 2015
Your Social Media Marketing is Under FDA`s Microscope
May 2015
What To Do If the Government Comes Knocking
May 2015
Health Canada`s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Foods and Beverages
Apr 2015
Foreign Corrupt Practices Act (FCPA) and International Anti-Bribery Course [Course -2]
Apr 2015
Foreign Corrupt Practices Act (FCPA) and International Anti-Bribery Course [Course-1]
Apr 2015
Occupy Movements, Free Speech Zones, Social Media, and More: Managing Student Activism on Your Campus
Apr 2015
Global and FDA Regulation of Electronic Cigarettes
Apr 2015
UDI Implementation
Apr 2015
Patients Suing Under HIPAA - Beware of New Laws and Risks
Apr 2015
Fundamentals of Administrative Law
Apr 2015
Private Placements and Red Flags to Look For
Apr 2015
Quality System Regulations for Devicemakers: A Regulatory Approach
Apr 2015
Guidelines to aid Fraud Risk Assessment and Internal Fraud Investigation
Apr 2015
Affordable Care Act New Tax Penalties: Impact on Individuals and Employers
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
Product Standards, Menthol and FDA`s Deeming Regulation
Mar 2015
Biomedical Software Regulation
Mar 2015
Immigration Law 101: 3 Key Issues for Compliance
Mar 2015
Preventing Faculty Discrimination with Case Law and Statistics
Mar 2015
How to Successfully Manage an FDA High Risk Inspection
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
Laboratory Developed Tests under FDA`s Thumb
Mar 2015
OSHA Inspections - Avoiding the 10 Most Common Mistakes
Mar 2015
Character of Reputation Risk: Risk or Just an Impact? Techniques for Effective Management.
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Labor and Employment Law Update
Mar 2015
Are Your Criminal Background Checks Legally Compliant?
Feb 2015
Ensuring Regulatory Compliance of Food Establishments
Feb 2015
Copyright and Fair Use Essentials for Faculty
Feb 2015
Corporate Governance Law 101 for Top Management to Monitor Compliance
Feb 2015
21 CFR 11 Compliance for Excel Spreadsheet
Feb 2015
Clinical Trial Liability Lawsuits
Feb 2015
The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs
Feb 2015
The FDA 510(k) and Q-Submission: Best Practices
Feb 2015
Postgraduate Diploma in Maritime Law
Jan 2015
FDA proposed changes to ISO 13485: and Medical Devices Quality Management Systems
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
HIPAA Omnibus Update - Tracking Down the Details
Jan 2015
A Systematic Approach To Writing Effective Standard Operating Procedures (SOPs)
Jan 2015
Nutrition Facts - NLEA and Beyond
Jan 2015
New AML Schemes to Detect and Prevent Fraudulent Transactions
Jan 2015
What is the harm in that? Risk Management 101
Jan 2015
Alternatives for Financing Export Sales
Jan 2015
Marine Salvage Law
Jan 2015
GAMP 5 as applied to FDA software validation - strategies to avoid warning letters
Jan 2015
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2015
Statistical Process Control (SPC)
Jan 2015
Clery Act Checklist: 10 Steps for Compliance
Jan 2015
FDA Decisions For IDE Clinical Investigations
Dec 2014
Regulatory Updates in China: APIs & Dossier Submissions
Dec 2014
cGMPs Beyond 21 CFR 110
Dec 2014
Developing an Efficient Relationship with FDA
Dec 2014
Peer Review and Potential Antitrust Liability
Dec 2014
Managing Product Recalls in Accordance with Part 806
Dec 2014
Clinical Trial Recruitment Methods and Metrics
Dec 2014
HIPAA Audits in 2015 - What to Expect and How to Prepare
Dec 2014
Certificate in Maritime Disputes & Arbitration
Nov 2014
FERPA Policy and Procedure Audit
Nov 2014
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements
Oct 2014
The Legal, Credit & Collection Environments in Brazil and Mexico
Oct 2014
Lets Get Back to the Basics of Withholding, Depositing and Reporting Federal Taxes
Oct 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
Compliance with the Americans with Disabilities Act
Oct 2014
Preparing for Year End and Year Beginning 2015
Oct 2014
Functions, Procedures and Permits of COFEPRIS & SENASICA - Agencies Regulating Fresh and Processed Foods in Mexico
Oct 2014
Implementing the Best Practices for FDA Inspection Preparation and Management
Oct 2014
Campus Safety`s Role in Title IX Investigations
Sep 2014
Preparing for Contract Negotiations
Sep 2014
FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs
Sep 2014
SOP and FDA Compliance
Aug 2014
How to handle a regulatory inspection to avoid FDA-483 issues
Aug 2014
Role of Analytical support during various audits - Regulatory and Non Regulatory
Aug 2014
Analyzing Your Biggest Data - Practical Text Mining for FDA-regulated Companies
Aug 2014
Food Laws and Regulations in Mexico
Aug 2014
Quality System Regulation: Equipment and Facilities Controls Subsystem
Aug 2014
FERPA Regulation Basics
Jul 2014
Detecting and Preventing Procure-to-Pay Fraud
Jul 2014
NAFTA Rules of Origin and Documentation
Jul 2014
21 CFR Part 11 Add-On Inspections by the FDA
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
How to Improve Service Levels in Startup, Small, Medium Sized Businesses with no Capital Investment
Jun 2014
Tax Levies and Creditor Garnishments: What Payroll Must Know to Stay in Compliance
Jun 2014
Postgraduate Diploma/Masters in European Union Law - From King`s College London
Jun 2014
Postgraduate Diploma/Masters in EU Competition Law - From King`s College London
Jun 2014
Preparing for FDA BIMO Inspection and Management
May 2014
Controversies around FDA`s Proposed Produce Safety Rules
May 2014
Strategies for Preserving Records with Long Retention Times
May 2014
When the Whistle Blows at Your Company
May 2014
Valuation Methods (U.S. Customs) for Imports into the United States
May 2014
Copyright Considerations for Using MOOCs in Your Courses
May 2014
Meet FDA Expectations for a Tougher Supplier Audit Program
May 2014
Certificate in Trade & Transport Law
Apr 2014
Implementing a Unique Device Identification (UDI) System - Issued on 2013
Apr 2014
Foundation Diploma in Admiralty Law & Practice
Mar 2014
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Mar 2014
Legal Issues Concerning Employees with Psychiatric Illnesses under the ADA and More!
Feb 2014
Legal and Effective Reference Checking and Education Verification
Feb 2014
RoHS2 Compliance for Medical Devices
Feb 2014
International Letters of Credit
Jan 2014
Mental health and stress in the workplace: Guidelines for meeting your accommodation duties
Jan 2014
The boomer generation: Proven solutions for managing an aging workforce
Jan 2014
Non-occupational disabilities: How far must an employer go in accommodation?
Jan 2014
FDA Inspection: Preparation and Management
Jan 2014
Private School Placements at Public Expense: IDEA Requirements & Case Law Update
Jan 2014
How to Deal with the IRS and other Governmental Agencies
Dec 2013
Preparing For The Management Occupancy Review (MOR)
Nov 2013
CBP’s Trade Transformation Initiatives
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
Pricing Contractor Delays
Oct 2013
Thorough and Complete Investigations and Follow-up - A Current Regulatory Expectation
Oct 2013
What AP (Accounts Payable) Needs to Know About Payroll and Vice Versa
Oct 2013
Premarket Review of New and Modified Tobacco Products
Oct 2013
Federal Sentencing Guidelines for Organizations (FSGO) Guidelines for your GRC System
Oct 2013
Charging for Investigational Drugs: Current Application of 21 CFR Part 312 and the Expanded Access Rules
Oct 2013
FERPA: When to Involve Legal Counsel and Leadership
Oct 2013
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Oct 2013
Child Support Garnishments: Withholding Procedures for
Oct 2013
Creating Effective Security Incident Response Procedures and Practices to Meet the Breach Notification Requirements
Aug 2013
Trial Preparation in Today’s Litigation Landscape – Webshop D
Aug 2013
Building an Effective Global Code of Conduct: The Eight Essential Elements of Successful Customization
Aug 2013
Key Drafting and Legal Research Primer – Webshop C
Aug 2013
E-Discovery Essentials: Advanced Theory and Best Practices– Webshop B
Aug 2013
Key Practice Management Updates: Preparing Discovery Plans, Expert Evidence, Costs Outlines and More – Webshop A
Aug 2013
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall
Aug 2013
New HIPAA Breach Notification Standards - Tougher Rules Require Risk Assessment
Jun 2013
Fundamentals of International Trade & Transport Law
Jun 2013
Anti-Kickback, Stark Laws and Marketing
May 2013
FDA Warning Letter Closeout Program
May 2013
Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates
Apr 2013
Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties
Apr 2013
Providing Assurance on GRC Activities
Apr 2013
510(k): Format and Contents
Apr 2013
Focus on Internal Control - Is your Company Ready for the New COSO?
Apr 2013
Complaint Handling in Compliance with FDA and ISO Regulations
Apr 2013
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
Mar 2013
The Corporate Director`s Fiduciary Role and Management`s Relationship
Mar 2013
Introduction to the US Department of Justice`s New FCPA Guidance Document - Key Takeaways & Future Planning
Mar 2013
FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance
Mar 2013
Defining Computer System Validation & Software Development Life-Cycle
Feb 2013
IPPF Internal Audit Standard 2120: Assessing the Effectiveness of Risk Management Processes
Feb 2013
14 CFR Part 21, Subpart K Requirements for Parts Manufacturer Approvals (PMA) - FAA Approval
Feb 2013
Purchasing and Supplier Controls in the Medical Device Industry
Feb 2013
How to Develop an Export Compliance Manual
Feb 2013
Complying with the Rules & Regulations Pertaining to Letters of Credit
Feb 2013
Conformance of Design History Files for Mature Medical Products
Feb 2013
What CEO`s Need and Expect from a Strategic HR Business Partnership
Feb 2013
Directors and Officers (D&O) Liability and Insurance - Everything a New Risk Manager Needs to Know
Jan 2013
Deviation Management System
Jan 2013
New Finalized HITECH Amendments to HIPAA - How Policies and Practices Must Be Changed
Jan 2013
Risk Status Oversight – New Risk Oversight Expectations and Financial Reporting Requirements
Jan 2013
Auditor Independence: Challenges and Opportunities
Jan 2013
SOX Compliance for Foreign-based Public Companies : Implementing US Corporate Governance and Internal Controls
Jan 2013
Trade Compliance Automation – Export Compliance Screening
Nov 2012
Ensuring Integrity and Security of Electronic Records for FDA Compliance
Nov 2012
FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements
Nov 2012
Obtaining an FDA Investigational Device Exemption - Webinar By GlobalCompliancePanel
Nov 2012
21 CFR Part 11 - Complete Manual for Compliance and Success
Nov 2012
Design Control for Medical Devices
Nov 2012
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Nov 2012
Avoiding an FDA Warning Letter with a Strong CAPA Program
Nov 2012
21 CFR Part 11: Complying with Part 11 Regulation - Understanding the Predicate Rule
Nov 2012
OSHA Ergonomics Compliance - What Every Organization Needs to Know
Nov 2012
Confidential Information and Human Resources
Oct 2012
Documentation and Investigative Report Writing
Oct 2012
Creating Material, Waste, and Personnel Flow Diagrams for Cleanrooms and Controlled Environments
Oct 2012
Developing and Maintaining Pre-marketing Master Regulatory Files
Oct 2012
Live webinar on Auditing Software Vendors & Service Providers for 21 CFR Part 11
Oct 2012
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits
Oct 2012
Title IV: Complying with New State Authorization Rules
Sep 2012
HITECH - Why It`s Important to Comply Now
Sep 2012
The New HIPAA Audit Protocol - What It Takes To Be Ready For An Audit
Sep 2012
FMEA and Risk Management for Medical Devices
Sep 2012
21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection
Sep 2012
Hazard Analysis – A practical guide
Sep 2012
Incorporating Six Sigma DMAIC into CAPA
Sep 2012
Key Steps to Avoid 483 Warning Letters & Remediation if you get one
Sep 2012
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485
Aug 2012
Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA
Aug 2012
Validation and Use of Excel Spreadsheets in Regulated Environments - Webinar By GlobalCompliancePanel
Aug 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
Preventing, Documenting, and Dealing with FMLA Abuse
Aug 2012
Business Law for Entrepreneurs
Aug 2012
Service Rig Move - National Safety Code Standard 9
Aug 2012
Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel
Aug 2012
Regulatory Complaint Handling, MDR`s & Recalls - Webinar By GlobalCompliancePanel
Aug 2012
Common Sense Water System Validation - Webinar By GlobalCompliancePanel
Aug 2012
Maximizing ROI on Each Compliance Effort - Webinar By ComplianceOnline
Jul 2012
Strategic Selection and Development of Immunogenicity Binding Methods
Jul 2012
Office Safety - Are you Protecting your Key Employees - Webinar By MentorHealth
Jul 2012
Auditing GRC Programs - Webinar By ComplianceOnline
Jul 2012
What Every FDA Regulated Company Needs to Know About its FDA District Office
Jul 2012
FDA’s Regulation of Veterinary Regenerative Medicine
Jun 2012
Lawful Hiring and Termination: Using Social Media as a Part in Decision Making
Jun 2012
Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations: One and a Half-day In-person Seminar
Jun 2012
Fundamentals of Nuclear Power
Jun 2012
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs - Webinar By ComplianceOnline
Jun 2012
Election Year Legal and Compliance - Webinar By ComplianceOnline
May 2012
What does Sarbanes-Oxley, Dodd-Frank and Hedging FOREX (derivatives) in a recessionary economy have in common, they’re all risk and compliance related!
May 2012
Import Compliance - How to Reduce Your Import Risks
May 2012
International Terms 2010 Rules By Compliance2go
May 2012
Improving Bank Compliance Management
May 2012
IT Risk Management – EU Laws and Regulations
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
Proper Documentation of Risk Management for Compliance with ISO 14971 - Webinar By GlobalCompliancePanel
May 2012
Applying GMP Quality Principles To Establish A Reduced Testing Program
May 2012
Physician Payment Sunshine Act and State Sunshine Law Compliance. Are you Prepared for the New Federal Requirements and Existing State Requirements?
Apr 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Complying with the EU Cookies Law Ecosystem
Apr 2012
Acceptance Activities in FDA QSR - Regulations and Warning Letters
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
California Environmental Regulations – Differences Between Federal EPA and State Requirements
Apr 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel
Mar 2012
Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go
Mar 2012
Ethical Hotlines, Whistleblowers and Compliance with the EU Data Privacy Laws & Regulations
Mar 2012
Changes in the EU Medical Device Directives; 2010 Modifications and the Recast of the MDD Directives - Webinar By GlobalCompliancePanel
Mar 2012
Reduce the Risks of Foreign Material Contamination - A Manufacturer`s Guide in Creating a Foreign Material Control
Mar 2012
How to Develop, Monitor and Effectively Communicate your Risk Control Strategy - Webinar By GlobalCompliancePanel
Mar 2012
Webinar: When Do You Need a 510K?
Mar 2012
Insurance Distribution Forum
Mar 2012
Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada
Mar 2012
Defending Against an OFAC Investigation
Feb 2012
Global Data Transfer Solutions – Complying with EU Laws & Regulations
Feb 2012
Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Feb 2012
Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA - Webinar By GlobalCompliancePanel
Feb 2012
Importing into the United States in Compliance with U.S. Customs & Border Protection (CBP)
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Record Keeping for a (Food) Recall: Keeping Records to Minimize the Affect of a Recall
Jan 2012
New Dietary Ingredients in the Regulatory Scheme
Jan 2012
FDA’s New Food Safety Law - What does It mean for everyone in the Global Food Chain
Jan 2012
An Introduction to the FDA New Drug Approval Process
Jan 2012
Introduction to FDA Good Documentation Practices
Jan 2012
International Financial Markets Law & Practice
Jan 2012
Social Networking: Legal Concerns for Employers in Employee Misbehavior & Conducting Background Checks
Jan 2012
FDA Compliant Handling of Out of Trend Results in Pharmaceutical Quality Control
Dec 2011
Accounting of Disclosures under HIPAA: What the Rules Require Today and What`s Changed by the Proposed Rule
Dec 2011
Live webcast on HOW TO MANAGE COMPLAINT FILES by Compliance2go
Dec 2011
GMP Annual Training
Dec 2011
Live webinar on Excel Spreadsheet Compliance with 21 CFR 11 by Compliance2go
Dec 2011
Foundation Diploma in Time Charterparties
Dec 2011
Foundation Diploma in Tanker Charterparties
Dec 2011
Document Approval, Control, and Distribution: How to Develop a Compliant, Cost Effective System By Compliance2go
Nov 2011
Performance Management: The Key to the Castle - Webinar By TrainHR
Nov 2011
Corporate Integrity Agreements Offer A Chance - Webinar By mentorhealth
Oct 2011
Draft Guidance for Device Industry and FDA - Postmarket Surveillance - Webinar By GlobalCompliancePanel
Oct 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
FDA`s Draft Guidance on Financial Disclosure by Clinical Investigators - Webinar By GlobalCompliancePanel
Oct 2011
Live webinar on HIPAA and EHRs - what your systems need to do so you can be in compliance with new rules by compliance2go
Oct 2011
Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalCompliancePanel
Oct 2011
Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel
Oct 2011
How to Identify Hazardous Wastes at the Work Place - Webinar By ComplianceOnline
Sep 2011
Documenting Payroll Procedures - Webinar By TrainHR
Sep 2011
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 - Webinar By GlobalCompliancePanel
Sep 2011
The Darker Side of Implementing Wellness Programs: Possible Career-Ending Decisions
Sep 2011
Good Laboratory Practice Regulations: Introduction and Strategies for Implementation
Sep 2011
A Guide to HACCP Validation and Verification for Food Manufacturers and Restaurants
Sep 2011
HIPAA Audits and Enforcement - new rules, new penalties, and a new audit program
Sep 2011
HIPAA Security Policies and Procedures: What you Need for Compliance
Sep 2011
FDA Validation Requirements - Webinar By ComplianceOnline
Sep 2011
Regulation of printing inks on food contact packaging materials in the US & EU
Sep 2011
Drug Master Files - Understanding and Meeting your Global Regulatory and Processing Responsibilities
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
A Rational Approach to Developing and Troubleshooting Dissolution Methods for a Variety of Purposes
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems
Sep 2011
Reliability Engineering Fundamentals for Medical Devices - Webinar By ComplianceOnline
Sep 2011
How to design A CAPA System that meets Compliance Requirements
Sep 2011
Ensuring Integrity and Security of Laboratory Data
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Eliminate the Confusion – Physician Quality Reporting System for Anesthesia Claims
Sep 2011
Why Nobody Believes the Numbers: The Secrets of Care Management Outcomes Measurement Revealed
Sep 2011
Master Validation Planning
Aug 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
Effective Hazard Analysis to meet FDA and ISO13485:2003 Risk Management Requirements
Aug 2011
Design, Planning and Conducting Effective Audits
Aug 2011
Risk Analysis Without Fear: Satisfying HIPAA & Meaningful Use Requirements for Privacy and Security
Aug 2011
Device Master Record & Device History Record
Aug 2011
Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11, Electronic Records, Signatures
Aug 2011
Why Post-market Pharmacovigilance trials are increasingly seen : What do they tell us and why are they important
Aug 2011
Design Reviews for Efficiency and Efficacy - Webinar By ComplianceOnline
Aug 2011
Full Day Virtual Seminar: Predicting Product Life Using Reliability Analysis Methods
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
Understanding the Difference: HIPAA Security Compliance Assessment v. HIPAA Security Risk Analysis
Aug 2011
Sterilization Options for Challenging Products - Webinar By ComplianceOnline
Aug 2011
W2s 1099s Independent Contractors? Protect Yourself with Proper Classification - Webinar By TrainHR
Aug 2011
How to Survive a DEA Inspection Series: Only Manufacturers and Distributors
Aug 2011
ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond
Aug 2011
Food Allergen Programs - Current Trends, Technologies and Risk Mitigation
Aug 2011
How to write Standard Operating Procedures (SOPS) & Work Instructions (Wis) that Meet and Exceed Compliance Requirements
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers
Aug 2011
Review and Implementation of USP <1058> Analytical Instrument Qualification
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
360 Degree Approach to Health Information Privacy - Webinar By ComplianceOnline
Aug 2011
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar by GlobalCompliancePanel
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Auditing the QC Microbiology Laboratory for FDA Compliance - Webinar By ComplianceOnline
Aug 2011
Information Security and Payment Card Rules: Complying with PCI and HIPAA, and Protecting Patient Payment Data
Aug 2011
Bioanalytical Methods Validation - Webinar By ComplianceOnline
Aug 2011
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar By ComplianceOnline
Aug 2011
How to manage an EPA inspection - Webinar By ComplianceOnline
Jul 2011
Full day Virtual Seminar on Pharmaceutical Stability - Webinar By ComplianceOnline
Jul 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials
Jul 2011
Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Jul 2011
The Investigational Medicinal Product Dossier (IMPD): EU`s CTA vs. FDA`s IND
Jul 2011
Full-day Virtual Seminar: IND Applications for the US FDA
Jul 2011
Cal/OSHA Enforcement and Defenses – Recent Changes in the Law
Jul 2011
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements
Jul 2011
Using the USP Effectively - Webinar By ComplianceOnline
Jul 2011
Key Concepts in OSHA Recordkeeping – 2.5 hrs comprehensive webinar
Jul 2011
How to Meet HIPAA-HITECH Encryption Requirements - Webinar By ComplianceOnline
Jul 2011
Validation of Analytical Methods and Procedures - Webinar By ComplianceOnline
Jul 2011
Eliminate the Confusion - Compliance for Anesthesia Services
Jul 2011
Navigating the new FDA world of Combination Products
Jun 2011
Master Production Record Requirements - Webinar By GlobalCompliancePanel
Jun 2011
Developing a Governance Risk Management and Compliance Strategy
Jun 2011
Information Security and Payment Card Rules: Protecting Patient Payment Data and Complying with PCI - Webinar By GlobalCompliancePanel
May 2011
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
May 2011
Information Security Risk Analysis: Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePanel
May 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
Apr 2011
FDA`s Revised 510(k) Premarket Notification Process
Apr 2011
Vendor/Supplier/CRO Compliance – Lessons Learned & Rules to Live By
Apr 2011
What Health Reform (and other Recent Changes) Means for Corporate Compliance
Mar 2011
International Terms 2010 Rules - ComplianceOnline Trade And Logistics Webinar
Mar 2011
Social Media in a Regulated Environment - ComplianceOnline Banking and Financial Training
Mar 2011
Process Validation: current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
Mar 2011
Internal Control for Smaller Entities - A Practical Cost - Effective Guide to Strengthening Internal Controls
Mar 2011
How to prepare for Increased OSHA penalties in
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
Foreign Corrupt Practices Act (FCPA) Webinar 2010
Feb 2011
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel
Feb 2011
Don`t RISK to ignore RISKS. Understanding ISO 14971
Feb 2011
Improve Your Audit Checklist - ComplianceOnline Quality Management Webinar
Feb 2011
Understanding and Implementing FDA’S 21 CFR Part 11
Feb 2011
Get Tough on Corrective Actions - ComplianceOnline Quality Management Webinar
Jan 2011
cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
Jan 2011
The Auditee Bill of Rights - ComplianceOnline Quality Management Webinar
Jan 2011
Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel
Jan 2011
HR Audits: A Critical Compliance Process - ComplianceOnline HR Webinar
Dec 2010
Preparing for a GSA Audit - ComplianceOnline GSA Webinar
Dec 2010
The Riskability Integration. – Integrating strategies and HR in EGRCM. Steps to leverage the impact of EGRCM mandates
Dec 2010
Accident Investigations and the Law – How to Find out what really happened - ComplianceOnline OSHA Webinar
Nov 2010
The multinational scopes of US and EU export controls and economic sanctions laws - ComplianceOnline Trade And Logistics Webinar
Nov 2010
Incoterms `Terms of Sale`
Nov 2010
Using Social Media in a FDA Compliant Manner
Oct 2010
Revamping the 510(k) Clearance Process-Understanding FDA`s Proposals - Webinar by GlobalCompliancePanel
Oct 2010
ComplianceOnline Webinar - Estimating Greenhouse Gas Emissions; Determining Your Carbon Footprint
Oct 2010
Using SLAs to Facilitate Enterprise and IT Governance, Risk Management and Compliance (GRC) - Webinar by GlobalCompliancePanel
Oct 2010
Introduction to Risk Management - Webinar by GlobalCompliancePanel
Oct 2010
How to Survive a DEA Audit or FIND=FINE - Webinar by GlobalCompliancePanel
Sep 2010
Managing Product Medical Device Recall Efficiently and Effectively - Webinar by GlobalCompliancePanel
Sep 2010
Development, Management, and Operation of an Effective Supplier and Internal Auditing System - Webinar by GlobalCompliancePanel
Sep 2010
Why Medical Device Companies Receive Warning Letters - Webinar by GlobalCompliancePanel
Sep 2010
Outsourced processes and ISO 9001:2008 - Webinar by GlobalCompliancePanel
Sep 2010
CAPA for Manufacturing, Financial Service Companies: Get it Right the Time (Efficient Process)
Sep 2010
Current dynamics of the current regulatory framework and the bills under consideration by Congress
Sep 2010
Environmental and Product Compliance - Sustainability - Webinar by GlobalCompliancePanel
Sep 2010
Preparing for FDA Inspections in a Changing Regulatory Environment - Webinar by GlobalCompliancePanel
Sep 2010
The Cosmetic-Cosmeceutical Distinction: Walking the Line in Developing Label Claims - Webinar by GlobalCompliancePanel
Sep 2010
Signal Detection and Data Mining - Webinar by GlobalCompliancePanel
Sep 2010
Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel
Sep 2010
Improving Sanitation Standard Operating Procedures in the Food Industry - Webinar by GlobalCompliancePanel
Sep 2010
Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel
Sep 2010
Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel
Sep 2010
Best Practices on Developing a Regulatory Framework to expand energy efficiency and renewable energy markets
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
Defining, Architecting and Managing Risk Assessments- Webinar by GlobalCompliancePanel
Aug 2010
NERC Compliance for Energy and Utility Companies – a risk intelligent approach
Aug 2010
Conduct Your Own Risk Assessments Following ISO Standard 31000/31010
Aug 2010

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